Uncovering Image-Driven Subtypes with Distinct Pathology and Clinical Course in Autopsy-Confirmed Four Repeat Tauopathies.

IF 8.1 1区 医学 Q1 CLINICAL NEUROLOGY
Ryota Satoh, Hiroaki Sekiya, Farwa Ali, Heather M Clark, Rene L Utianski, Joseph R Duffy, Mary M Machulda, Dennis W Dickson, Keith A Josephs, Jennifer L Whitwell
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Abstract

Objectives: The four-repeat (4R) tauopathies are a group of neurodegenerative diseases, including progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), and globular glial tauopathy (GGT). This study aimed to characterize spatiotemporal atrophy progression using structural magnetic resonance imaging (MRI) and to examine its relationship with clinical course and neuropathology in a cohort of autopsy-confirmed 4R tauopathies.

Methods: The study included 85 autopsied patients (54 with PSP, 28 with CBD, and 3 with GGT) who underwent multiple 3T MRI scans, as well as neuropsychological, neurological, and speech/language examinations, and standardized postmortem neuropathological evaluations. An unsupervised machine-learning algorithm, Subtype and Stage Inference (SuStaIn), was applied to the cross-sectional brain volumes to estimate spatiotemporal atrophy patterns and data-driven subtypes and stages in each patient. The relationships among estimated subtypes, pathological diagnoses, and longitudinal changes in clinical testing were examined.

Results: The SuStaIn algorithm identified 2 distinct subtypes: (1) the subcortical subtype, in which atrophy progresses from the midbrain to the cortex, and (2) the cortical subtype, in which atrophy progresses from the frontal cortex to the subcortical regions. The subcortical subtype was more associated with typical PSP, whereas the cortical subtype was more associated with atypical PSP with a cortical distribution of pathology and CBD (p < 0.001). The cortical subtype had a faster rate of change on the PSP Rating Scale than the subcortical subtype (p < 0.05).

Interpretation: SuStaIn analysis revealed 2 MRI-driven subtypes with distinct spatiotemporal atrophy patterns, clinical courses, and neuropathology. Our findings contribute to a comprehensive and improved understanding of disease progression and its relationship to tau pathology in 4R tauopathies. ANN NEUROL 2025.

揭示尸检证实的四种重复tau病变中具有独特病理和临床过程的图像驱动亚型。
目的:四重复(4R) tau病是一组神经退行性疾病,包括进行性核上性麻痹(PSP)、皮质基底变性(CBD)和global glial tau病(GGT)。本研究旨在利用结构磁共振成像(MRI)表征时空萎缩的进展,并研究其与尸检证实的4R tau病变的临床病程和神经病理学的关系。方法:研究纳入了85例尸检患者(54例PSP, 28例CBD, 3例GGT),他们接受了多次3T MRI扫描、神经心理学、神经学和言语/语言检查,以及标准化的死后神经病理学评估。一种无监督的机器学习算法,亚型和阶段推断(SuStaIn),应用于横断面脑容量,以估计每个患者的时空萎缩模式和数据驱动的亚型和阶段。研究了估计亚型、病理诊断和临床试验的纵向变化之间的关系。结果:SuStaIn算法确定了2种不同的亚型:(1)皮层下亚型,萎缩从中脑向皮层进展;(2)皮层亚型,萎缩从额叶皮层向皮层下区域进展。皮层下亚型与典型的PSP更相关,而皮层亚型与非典型PSP更相关,具有皮层分布的病理和CBD (p)解释:SuStaIn分析揭示了2种mri驱动的亚型,具有不同的时空萎缩模式、临床病程和神经病理学。我们的研究结果有助于全面和更好地了解4R tau病变的疾病进展及其与tau病理学的关系。Ann neurol 2025。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Neurology
Annals of Neurology 医学-临床神经学
CiteScore
18.00
自引率
1.80%
发文量
270
审稿时长
3-8 weeks
期刊介绍: Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.
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